SkeletonPlanner— 510(k) K260206
Substantially EquivalentUPlanner B.V. - Presurgeo
FDA 510(k) clearance K260206 for SkeletonPlanner, Substantially Equivalent on 2026-07-15. Applicant: UPlanner B.V. - Presurgeo.
Clearance details
- Applicant
- UPlanner B.V. - Presurgeo
- Product code
- Code QIH
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Vreeland, NL
Data sourced from openFDA. This site is unofficial and independent of the FDA.